EP0048429B1 - Cooling fluid containing anti-corrosive and anti-cavitation additives - Google Patents
Cooling fluid containing anti-corrosive and anti-cavitation additives Download PDFInfo
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- EP0048429B1 EP0048429B1 EP81107255A EP81107255A EP0048429B1 EP 0048429 B1 EP0048429 B1 EP 0048429B1 EP 81107255 A EP81107255 A EP 81107255A EP 81107255 A EP81107255 A EP 81107255A EP 0048429 B1 EP0048429 B1 EP 0048429B1
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- carbon atoms
- hydrogen
- cavitation
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- 239000000654 additive Substances 0.000 title description 6
- 239000012809 cooling fluid Substances 0.000 title 1
- 238000005260 corrosion Methods 0.000 claims abstract description 27
- 230000007797 corrosion Effects 0.000 claims abstract description 26
- 239000000110 cooling liquid Substances 0.000 claims abstract description 23
- 239000003112 inhibitor Substances 0.000 claims abstract description 21
- 230000002401 inhibitory effect Effects 0.000 claims abstract description 19
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims abstract description 18
- 150000001875 compounds Chemical class 0.000 claims abstract description 15
- 150000005846 sugar alcohols Polymers 0.000 claims abstract description 7
- -1 alkylene glycols Chemical class 0.000 claims description 42
- 125000004432 carbon atom Chemical group C* 0.000 claims description 36
- 229910052739 hydrogen Inorganic materials 0.000 claims description 21
- 239000001257 hydrogen Substances 0.000 claims description 19
- 239000007788 liquid Substances 0.000 claims description 19
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 11
- 229910052783 alkali metal Inorganic materials 0.000 claims description 9
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical group C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 8
- 125000000217 alkyl group Chemical group 0.000 claims description 8
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 5
- 239000005977 Ethylene Substances 0.000 claims description 4
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical group [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 4
- 150000001340 alkali metals Chemical group 0.000 claims description 4
- 150000005840 aryl radicals Chemical class 0.000 claims description 4
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 4
- 150000003254 radicals Chemical class 0.000 claims description 4
- 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 claims description 3
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical group C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 3
- 229910052910 alkali metal silicate Inorganic materials 0.000 claims description 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 3
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical compound [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 claims description 3
- 229910052700 potassium Chemical group 0.000 claims description 3
- 239000011591 potassium Chemical group 0.000 claims description 3
- 229910052708 sodium Inorganic materials 0.000 claims description 3
- 239000011734 sodium Chemical group 0.000 claims description 3
- 125000003944 tolyl group Chemical group 0.000 claims description 3
- 150000001565 benzotriazoles Chemical class 0.000 claims description 2
- 150000003839 salts Chemical class 0.000 claims description 2
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical group CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims 1
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims 1
- 229910001963 alkali metal nitrate Inorganic materials 0.000 claims 1
- 229910000318 alkali metal phosphate Inorganic materials 0.000 claims 1
- 239000000470 constituent Substances 0.000 claims 1
- 125000006353 oxyethylene group Chemical group 0.000 claims 1
- 238000002485 combustion reaction Methods 0.000 abstract description 6
- 150000002334 glycols Chemical class 0.000 abstract description 4
- 239000003795 chemical substances by application Substances 0.000 abstract description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 13
- 229910052799 carbon Inorganic materials 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- 238000001816 cooling Methods 0.000 description 10
- 239000000203 mixture Substances 0.000 description 8
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 7
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 7
- 238000012360 testing method Methods 0.000 description 7
- 239000003513 alkali Substances 0.000 description 6
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 5
- 239000002826 coolant Substances 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- 230000033228 biological regulation Effects 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 150000002431 hydrogen Chemical group 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 229910000838 Al alloy Inorganic materials 0.000 description 3
- 239000004215 Carbon black (E152) Substances 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 239000002518 antifoaming agent Substances 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 150000002739 metals Chemical class 0.000 description 3
- XUJLWPFSUCHPQL-UHFFFAOYSA-N 11-methyldodecan-1-ol Chemical compound CC(C)CCCCCCCCCCO XUJLWPFSUCHPQL-UHFFFAOYSA-N 0.000 description 2
- BWDBEAQIHAEVLV-UHFFFAOYSA-N 6-methylheptan-1-ol Chemical compound CC(C)CCCCCO BWDBEAQIHAEVLV-UHFFFAOYSA-N 0.000 description 2
- PLLBRTOLHQQAQQ-UHFFFAOYSA-N 8-methylnonan-1-ol Chemical compound CC(C)CCCCCCCO PLLBRTOLHQQAQQ-UHFFFAOYSA-N 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 2
- 239000006260 foam Substances 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
- 239000007769 metal material Substances 0.000 description 2
- 238000002604 ultrasonography Methods 0.000 description 2
- 238000005303 weighing Methods 0.000 description 2
- 230000004580 weight loss Effects 0.000 description 2
- BPRJQFIHEGORJE-UHFFFAOYSA-N 2-(1-hydroxypropan-2-yloxy)propan-1-ol 1-(2-hydroxypropoxy)propan-2-ol Chemical compound CC(O)COCC(C)O.CC(CO)OC(C)CO BPRJQFIHEGORJE-UHFFFAOYSA-N 0.000 description 1
- LCZVSXRMYJUNFX-UHFFFAOYSA-N 2-[2-(2-hydroxypropoxy)propoxy]propan-1-ol Chemical compound CC(O)COC(C)COC(C)CO LCZVSXRMYJUNFX-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- 229910001060 Gray iron Inorganic materials 0.000 description 1
- 239000004440 Isodecyl alcohol Substances 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 230000002528 anti-freeze Effects 0.000 description 1
- 150000001555 benzenes Chemical class 0.000 description 1
- 150000001558 benzoic acid derivatives Chemical class 0.000 description 1
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 1
- 239000012964 benzotriazole Substances 0.000 description 1
- 150000001642 boronic acid derivatives Chemical class 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 125000002960 margaryl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 150000002826 nitrites Chemical class 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 230000010355 oscillation Effects 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000002958 pentadecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- NVBFHJWHLNUMCV-UHFFFAOYSA-N sulfamide Chemical class NS(N)(=O)=O NVBFHJWHLNUMCV-UHFFFAOYSA-N 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- 125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K5/00—Heat-transfer, heat-exchange or heat-storage materials, e.g. refrigerants; Materials for the production of heat or cold by chemical reactions other than by combustion
- C09K5/20—Antifreeze additives therefor, e.g. for radiator liquids
Definitions
- the invention relates to a corrosion-inhibiting and cavitation-inhibiting cooling liquid composed of at least one polyhydric alcohol from the group of glycerol, alkylene glycols having 2 to 6 carbon atoms and oxalkylene glycols of oxethylene and / or oxpropylene. with a total of 4 to 12 carbon atoms as the main component and from at least one corrosion inhibitor and at least one cavitation inhibitor in an effective amount in each case.
- Water is generally used to cool technical equipment such as heat engines, pumps and the like and, in the event of a risk of frost, polyhydric alcohols such as ethylene glycol, propylene glycol and glycerol or mixtures of water and polyhydric alcohols.
- polyhydric alcohols such as ethylene glycol, propylene glycol and glycerol or mixtures of water and polyhydric alcohols.
- various auxiliaries are added in an effective amount, preferably corrosion- and cavitation-inhibiting compounds, optionally also pH stabilizers and anti-foaming agents.
- the cooling liquids should provide a good cooling effect and, on the other hand, should not cause any damage to the cooling system, which generally consists of metallic materials, in particular no damage by corrosion and cavitation.
- cavitation damage is generally shown in the form of hollowing out or cavity formation, whereby the surface of the material is roughened and destroyed like a sponge.
- cooling liquids for internal combustion engines which essentially consist of a) water and / or alkylene glycols (antifreeze) as the main component, b) an effective amount of conventional anti-corrosion agents and c) one effective amount of anti-cavitation compounds exist.
- the cavitation-inhibiting compounds used are higher alcohols, preferably monohydric and dihydric alcohols having 6 to 20 carbon atoms, polyvinylpyrrolidone with an average molecular weight of 300,000 to 1,000,000 and reaction products of organic compounds carrying active hydrogen atoms with an alkylene oxide, preferably oxalkylene glycols.
- These cooling liquids have a satisfactory corrosion inhibition.
- the corrosion inhibitors used are compatible with the main component and they also give relatively good corrosion protection. However, the behavior and the effect of the cavitation-inhibiting compounds leave something to be desired.
- Cavitation-inhibiting substances are primarily intended to provide very good protection against cavitation, regardless of the type of metallic material.
- automobile engines in particular have increasingly been manufactured from light metal, preferably from aluminum or aluminum alloys.
- light metals are far more at risk of cavitation than heavy metals, for example gray cast iron.
- Cavitation-inhibiting substances must therefore be particularly effective against light metals. In addition, they should also meet a number of other requirements.
- This liquid only has a corrosion-inhibiting effect if the metal surface with which it comes into contact during intended use has been passivated or phosphated beforehand. Because of the use of oil as a mixture component, this cooling liquid is not homogeneous and has the associated disadvantages.
- the object of the invention is to provide a corrosion-inhibiting and cavitation-inhibiting cooling liquid, in particular for internal combustion engines, which guarantees excellent protection against corrosion and cavitation even against light metals, preferably aluminum and aluminum alloys, without pretreatment, which is stable, i.e. homogeneous Represents liquid at both low and high temperatures, does not foam significantly and is easy to handle.
- alkyl and alkenyl radicals can be straight-chain or branched, they are preferably straight-chain.
- alkenyl radicals those with 1 to 2 double bonds are preferred.
- R and R 2 are, for example: decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl and stearyl or mixtures thereof, preferably those with C 12 -C 18 -alkyl radicals.
- R and R 2 in formulas 1 and 11 also represent such mixtures, for example the C 12 to C 21 hydrocarbon mixture of C 12 2%, C 13 5%, C 14 1 12%, C 15 18%, C 16 17%, C 17 16%, C1 8 12%, C 19 9% , C 20 6%, and C 21 3% by weight, with 47% by weight of naphthenes and 53% by weight of paraffins.
- a preferred corrosion inhibitor consists essentially of alkali metal laborate in an amount of 0.5 to 5% by weight, alkali metal benzate in an amount of 0.5 to 5% by weight, alkali metal nitrite in an amount of 0.1 to 0.6% by weight .-%, alkali nitrate in one of 0.05 to 0.5 wt .-%, alkali silicate in an amount of 0.01 to 0.5 wt .-% and benzotriazole in an amount of 0.01 to 0.5 wt .-%, weight percent based on the weight of the liquid.
- the amount of corrosion inhibitor in the cooling liquid according to the invention is 2 to 10% by weight, preferably 3 to 7% by weight, based on the weight of the liquid.
- the cooling liquid according to the invention is produced simply by mixing the individual components together. This can be done, for example, in a container equipped with a stirrer.
- the cooling liquid according to the invention is characterized by a surprisingly high cavitation inhibitory and corrosion-inhibiting effect. Since the individual components of the liquid are compatible with one another, it is stable even at relatively high and low temperatures. It shows low foaming, especially when using anti-foaming agents.
- the coolant according to the invention is versatile. It is preferably used in the cooling circuit of heat engines and pumps, in particular internal combustion engines. It is expediently diluted with water so that it is present in a concentration of 20 to 45% by volume.
- R represents a C 12-21 hydrocarbon mixture of C 12 2%, C, 3 5%, C 14 12%, C 15 18%, C 16 17%, C 17 16%, C 18 12%, C 19 9%, C 20 6% and C 21 3% by weight, the proportion of naphthenes being 47% by weight and that of paraffins 53% by weight.
- a cooling liquid according to the invention was produced by mixing the following components:
- a cooling liquid according to the invention was produced by mixing the following components:
- a cooling liquid according to the invention was produced by mixing the following components:
- This cooling liquid consisted of the components of Example 1, but without the addition of compound No. 1 according to the invention:
- the cooling liquids according to Examples 1 to 8 were tested for their anticavitative activity in accordance with the regulations of the Research Association for Combustion Engines EV Frankfurt / Main, Federal Republic of Germany. These regulations are contained in the guidelines for «Prü the suitability of coolant additives for the coolants of internal combustion engines » booklet R 315, year 1977.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Combustion & Propulsion (AREA)
- Thermal Sciences (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Preventing Corrosion Or Incrustation Of Metals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Description
Die Erfindung betrifft eine korrosionsinhibierende und kavitationsinhibierende Kühlflüssigkeit aus mindestens einem mehrwertigen Alkohol aus der Gruppe von Glycerin, Alkylenglykolen mit 2 bis 6 C-Atomen und Oxalkylenglykolen des Oxethylens und/oder Oxpropylens. mit insgesamt 4 bis 12 C-Atomen als Hauptbestandteil und aus mindestens einem korrosionsinhibitor und mindestens einem Kavitationsinhibitor in einer jeweils wirksamen Menge.The invention relates to a corrosion-inhibiting and cavitation-inhibiting cooling liquid composed of at least one polyhydric alcohol from the group of glycerol, alkylene glycols having 2 to 6 carbon atoms and oxalkylene glycols of oxethylene and / or oxpropylene. with a total of 4 to 12 carbon atoms as the main component and from at least one corrosion inhibitor and at least one cavitation inhibitor in an effective amount in each case.
Zum Kühlen von technischen Einrichtungen wie Wärmekraftmaschinen, Pumpen und dergleichen werden im allgemeinen Wasser und im Falle von Frostgefahr mehrwertige Alkohole wie Ethylenglykol, Propylenglykol und Glycerin oder Mischungen von Wasser und mehrwertigen Alkoholen eingesetzt. Zur Erreichung einer optimalen Funktion werden verschiedene Hilfsmittel in wirksamer Menge, vorzugsweise korrosions- und kavitationshemmende Verbindungen, gegebenenfalls auch pH-Wert-Stabilisatoren und Antischaummittel, zugesetzt. Die Kühlflüssigkeiten sollen nämlich einerseits eine gute Kühlwirkung liefern und andererseits keine Schädigung an dem in der Regel aus metallischen Werkstoffen bestehenden Kühlsystem hervorrufen, insbesondere keine Schädigung durch Korrosion und Kavitation.Water is generally used to cool technical equipment such as heat engines, pumps and the like and, in the event of a risk of frost, polyhydric alcohols such as ethylene glycol, propylene glycol and glycerol or mixtures of water and polyhydric alcohols. To achieve optimal function, various auxiliaries are added in an effective amount, preferably corrosion- and cavitation-inhibiting compounds, optionally also pH stabilizers and anti-foaming agents. On the one hand, the cooling liquids should provide a good cooling effect and, on the other hand, should not cause any damage to the cooling system, which generally consists of metallic materials, in particular no damage by corrosion and cavitation.
Während die Schädigung des Werkstoffes durch Korrosion auf einem rein chemischen Angriff des Werkstoffes beruht, spielen bei der Kavitation auch physikalische Erscheinungen eine wesentliche Rolle. Die Kavitationsschädigung zeigt sich im allgemeinen in Form von Aushöhlung oder Hohlraumbildung, wobei die Oberfläche des Werkstoffes aufgerauht und schwammartig zerstört wird.While the damage to the material due to corrosion is based on a purely chemical attack of the material, physical phenomena also play an important role in cavitation. The cavitation damage is generally shown in the form of hollowing out or cavity formation, whereby the surface of the material is roughened and destroyed like a sponge.
Aus den deutschen Patentschriften 1 239 137, 1 239 138 und 1 263 398 sind Kühlflüssigkeiten für Verbrennungsmotoren bekannt, die im wesentlichen aus a) Wasser und/oder Alkylenglykolen (Frostschutzmittel) als Hauptbestandteil, b) einer wirksamen Menge von üblichen Antikorrosionsmitteln und c) einer wirksamen Menge von kavitationshemmende Verbindungen bestehen. Als kavitationshemmende Verbindungen werden höhere Alkohole, vorzugsweise einwertige und zweiwertige Alkohole mit 6 bis 20 Kohlenstoffatomen, Polyvinylpyrrolidon mit einem mittleren Molekulargewicht von 300 000 bis 1 000 000 und Umsetzungsprodukte von aktive Wasserstoffatome tragenden organischen Verbindungen mit einem Alkylenoxid, vorzugsweise Oxalkylenglykole, eingesetzt. Diese Kühlflüssigkeiten weisen eine zufriedenstellende Korrosionsinhibierung auf. Die verwendeten Korrosionsinhibitoren sind mit der Hauptkomponente verträglich, und sie geben auch einen relativ guten Korrosionsschutz. Dagegen lassen aber das Verhalten und die Wirkung der kavitationshemmenden Verbindungen zu wünschen übrig.From the German patents 1 239 137, 1 239 138 and 1 263 398 cooling liquids for internal combustion engines are known which essentially consist of a) water and / or alkylene glycols (antifreeze) as the main component, b) an effective amount of conventional anti-corrosion agents and c) one effective amount of anti-cavitation compounds exist. The cavitation-inhibiting compounds used are higher alcohols, preferably monohydric and dihydric alcohols having 6 to 20 carbon atoms, polyvinylpyrrolidone with an average molecular weight of 300,000 to 1,000,000 and reaction products of organic compounds carrying active hydrogen atoms with an alkylene oxide, preferably oxalkylene glycols. These cooling liquids have a satisfactory corrosion inhibition. The corrosion inhibitors used are compatible with the main component and they also give relatively good corrosion protection. However, the behavior and the effect of the cavitation-inhibiting compounds leave something to be desired.
Kavitationshemmende Substanzen sollen vor allem einen sehr guten Schutz gegen Kavitation liefern, und zwar unabhängig von der Art des metallischen Werkstoffes. In neuerer Zeit werden insbesondere die Automobilmotoren zunehmend aus leichtmetall, vorzugsweise aus Aluminium oder Aluminiumlegierungen, hergestellt. Leichtmetalle sind aber weit mehr kavitationsgefährdet als Schwermetalle, beispielsweise Grauguss. Kavitationshemmende Substanzen müssen daher insbesondere auch gegenüber Leichtmetallen wirksam sein. Darüber hinaus sollten sie auch noch eine Reihe weiterer Forderungen erfüllen. Darunter sind insbesondere zu nennen: genügende Löslichkeit in Wasser und in ein- und mehrwertigen Alkoholen, vorzugsweise Glycerin, Alkylenglykolen und Oxalkylenglykolen; Verträglichkeit mit den verwendeten Korrosionsinhibitoren; keine oder keine nennenswerte Entmischungsneigung sowohl bei tiefen als auch bei höheren Temperaturen; keine oder keine nennenswerte Neigung zur Schaumbildung; und Inertheit gegenüber Kunststoffen, vorzugsweise gegenüber Elastomeren.Cavitation-inhibiting substances are primarily intended to provide very good protection against cavitation, regardless of the type of metallic material. In recent times, automobile engines in particular have increasingly been manufactured from light metal, preferably from aluminum or aluminum alloys. However, light metals are far more at risk of cavitation than heavy metals, for example gray cast iron. Cavitation-inhibiting substances must therefore be particularly effective against light metals. In addition, they should also meet a number of other requirements. These include in particular: sufficient solubility in water and in monohydric and polyhydric alcohols, preferably glycerol, alkylene glycols and oxalkylene glycols; Compatibility with the corrosion inhibitors used; no or no significant tendency to segregate both at low and at higher temperatures; no or no appreciable tendency to foam; and inertness towards plastics, preferably towards elastomers.
Aus den beiden französischen Patentschriften 2 236 018 und 2 249 181 sind Verbindungen der nachstehenden allgemeinen Formel bekannt,
Die Aufgabe der Erfindung besteht nun darin, eine korrosionsinhibierende und kavitationsinhibierende Kühlflüssigkeit, insbesondere für Verbrennungsmotoren, zu schaffen, die einen hervorragenden Korrosions- und Kavitationsschutz auch gegenüber Leichtmetallen, vorzugsweise Aluminium und Aluminiumlegierungen, ohne eine Vorbehandlung gewährleistet, die stabil ist, dass heisst eine homogene Flüssigkeit sowohl bei tiefen als auch bei hohen Temperaturen darstellt, nicht nennenswert schäumt und leicht zu handhaben ist.The object of the invention is to provide a corrosion-inhibiting and cavitation-inhibiting cooling liquid, in particular for internal combustion engines, which guarantees excellent protection against corrosion and cavitation even against light metals, preferably aluminum and aluminum alloys, without pretreatment, which is stable, i.e. homogeneous Represents liquid at both low and high temperatures, does not foam significantly and is easy to handle.
Diese Aufgabe wird bei der eingangs genannten Kühlflüssigkeit dadurch gelöst, dass der Korrosionsinhibitor eine Verbindung aus der Gruppe der Alkaliborate, Alkalibenzoate, Alkalinitrite, Alkalinitrate, Alkalisilicate, Alkaliphosphate, Benztriazole und Alkanolamine und deren Salze ist und der Kavitations- inhibitor eine Verbindung der Formel 1
- R einen Alkyl- oder Alkenylrest mit 4 bis 25 C-Atomen oder einen Arylrest mit 6 bis 10 C-Atomen,
- R1 Wasserstoff oder einen Alkylrest mit 1 bis 4 C-Atomen,
- M Wasserstoff oder ein Alkalimetall, und
- x eine ganze Zahl von 1 bis 5;
oder der Formel 11 - R2 einen Alkyl- oder Alkenylrest mit 4 bis 25 C-Atomen,
- R3 einen Alkylenrest mit 2 bis 4 C-Atomen,
- n eine ganze Zahl von 1 bis 10,
- R4 Wasserstoff, einen Alkylrest mit 1 bis 4 C-Atomen oder einen Rest -(OR5)mH, worin R5 ein Alkylenrest mit 2 bis 4 C-Atomen und m eine ganze Zahl von 1 bis 10 ist,
wobei die Menge an Korrosionsinhibitor 2 bis 10 Gew.-% und die Menge an Kavitationsinhibitor 0,01 bis 3,0 Gew.-% beträgt, Gewichtsprozente jeweils bezogen auf das Gewicht der Flüssigkeit.This problem is solved in the case of the cooling liquid mentioned at the outset in that the corrosion inhibitor is a compound from the group of the alkali borates, alkali benzoates, alkali nitrites, alkali nitrates, alkali silicates, alkali phosphates, benzotriazoles and alkanolamines and their salts and the cavitation inhibitor is a compound of the formula 1
- R is an alkyl or alkenyl radical with 4 to 25 C atoms or an aryl radical with 6 to 10 C atoms,
- R 1 is hydrogen or an alkyl radical having 1 to 4 carbon atoms,
- M is hydrogen or an alkali metal, and
- x is an integer from 1 to 5;
or formula 11 - R 2 is an alkyl or alkenyl radical having 4 to 25 carbon atoms,
- R 3 is an alkylene radical with 2 to 4 carbon atoms,
- n is an integer from 1 to 10,
- R 4 is hydrogen, an alkyl radical with 1 to 4 C atoms or a radical - (OR 5 ) m H, where R 5 is an alkylene radical with 2 to 4 C atoms and m is an integer from 1 to 10,
the amount of corrosion inhibitor being 2 to 10% by weight and the amount of cavitation inhibitor being 0.01 to 3.0% by weight, percentages by weight in each case based on the weight of the liquid.
In Formel 1 bedeuten
- R vorzugsweise einen Alkylrest mit 8 bis 20 C-Atomen insbesondere mit 12 bis 18 C-Atomen, oder einen Arylrest aus der Gruppe von Phenyl, Benzyl, Phenethyl und Tolyl, insbesondere Phenyl,
- R1 vorzugsweise Wasserstoff oder einen Alkylrest mit 1 bis 3 C-Atomen, insbesondere Wasserstoff oder den Methylrest, und
- M vorzugsweise Wasserstoff, Natrium oder Kalium.
- R preferably an alkyl radical with 8 to 20 carbon atoms, in particular with 12 to 18 carbon atoms, or an aryl radical from the group of phenyl, benzyl, phenethyl and tolyl, in particular phenyl,
- R 1 is preferably hydrogen or an alkyl radical having 1 to 3 carbon atoms, in particular hydrogen or the methyl radical, and
- M preferably hydrogen, sodium or potassium.
In Formel II bedeuten
- R2 vorzugsweise einen Alkylrest mit 8 bis 20 C-Atomen, insbesondere mit 12 bis 18 C-Atomen,
- R3 vorzugsweise einen Ethylen- und/oder Propylenrest, insbesondere den Ethylenrest,
- n vorzugsweise eine ganze Zahl von 2 bis 5,
- R4 vorzugsweise Wasserstoff, einen Alkylrest mit 1 bis 3 C-Atomen, insbesondere Wasserstoff oder -CH3, oder einen Rest -(OR5)mH, worin R5 ein Ethylen- und/oder Propylenrest, insbesondere der Ethylenrest, und m eine ganze Zahl von 2 bis 5 ist. Die Summe von n und m beträgt im allgemeinen 4 bis 20, vorzugsweise 4 bis 10.
- R 2 is preferably an alkyl radical with 8 to 20 C atoms, in particular with 12 to 18 C atoms,
- R 3 is preferably an ethylene and / or propylene radical, in particular the ethylene radical,
- n is preferably an integer from 2 to 5,
- R4 is preferably hydrogen, an alkyl radical having 1 to 3 carbon atoms, in particular hydrogen or -CH 3 , or a radical - (OR 5 ) m H, where R 5 is an ethylene and / or propylene radical, in particular the ethylene radical, and is an integer from 2 to 5. The sum of n and m is generally 4 to 20, preferably 4 to 10.
In Formel I und 11 können die Alkyl- und Alkenylreste geradkettig oder verzweigt sein, sie sind vorzugsweise geradkettig. Von den Alkenylresten sind diejenigen mit 1 bis 2 Doppelbindungen bevorzugt.In formulas I and 11, the alkyl and alkenyl radicals can be straight-chain or branched, they are preferably straight-chain. Of the alkenyl radicals, those with 1 to 2 double bonds are preferred.
Vorteilhafte Vertreter von R und R2 sind beispielsweise: Decyl, Undecyl, Dodecyl, Tridecyl, Tetradecyl, Pentadecyl, Hexadecyl, Heptadecyl und Stearyl oder Gemische davon, vorzugsweise solche mit C12- bis C18-Alkylresten. Da bei der Herstellung von Verbindungen gemäss Formel und 11 auch von Kohlenwasserstoffgemischen ausgegangen wird, wie sie beispielsweise bei der Fischer-Tropsch-Synthese oder bei der Erdölaufbereitung als Fraktionen anfallen, stellen R und R2 in Formel 1 und 11 auch derartige Gemische dar, beispielsweise das C12- bis C21-Kohlenwasserstoffgemisch aus C12 2%, C13 5%, C14 1 12%, C15 18%, C16 17%, C17 16%, C18 12%, C19 9%, C20 6%, und C21 3 Gew.-%, mit 47 Gew.-% an Naphthenen und 53 Gew.-% an Paraffinen.Advantageous representatives of R and R 2 are, for example: decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl and stearyl or mixtures thereof, preferably those with C 12 -C 18 -alkyl radicals. Since the preparation of compounds according to formula and 11 also starts from hydrocarbon mixtures, such as those obtained as fractions in Fischer-Tropsch synthesis or in petroleum processing, R and R 2 in formulas 1 and 11 also represent such mixtures, for example the C 12 to C 21 hydrocarbon mixture of C 12 2%, C 13 5%, C 14 1 12%, C 15 18%, C 16 17%, C 17 16%, C1 8 12%, C 19 9% , C 20 6%, and C 21 3% by weight, with 47% by weight of naphthenes and 53% by weight of paraffins.
Der mehrwertige Alkohol (Komponente A) der erfindungsgemässen Kühlflüssigkeit ist vorzugsweise Glycerin, ein Alkylenglykol mit 2 bis 4 C-Atomen und/oder ein Oxalkylenglykol aus der Gruppe von Diethylenglykol, Triethylenglykol, Dipropylenglykol und Tripropylenglykol.
- Besonders bevorzugt ist Monoethylenglykol, Diethylenglykol, Monopropylenglykol und/oder Dipropylenglykol.
- Die Komponente A bildet den Hauptbestandteil der neuen Kühlflüssigkeit. Die Menge beträgt im allgemeinen 87 bis 98 Gew.-%, vorzugsweise 92 bis 97 Gew.-%, bezogen auf das Gewicht der Flüssigkeit (Gesamtgewicht).
- Monoethylene glycol, diethylene glycol, monopropylene glycol and / or dipropylene glycol is particularly preferred.
- Component A is the main component of the new coolant. The amount is generally 87 to 98% by weight, preferably 92 to 97% by weight, based on the weight of the liquid (total weight).
Da die erfindungsgemäss einzusetzenden Korrosionsinhibitoren (Komponente B) im allgemeinen auch pH-Wert-stabilisierend wirken, sind eigene Puffersubstanzen nicht mehr erforderlich. In der Regel wird eine Mischung aus den genannten Korrosionsinhibitoren verwendet. Ein bevorzugter Korrosionsinhibitor besteht im wesentlichen aus Alkalitetraborat in einer Menge von 0,5 bis 5 Gew.-%, Alkalibenzoat in einer Menge von 0,5 bis 5 Gew.-%, Alkalinitrit in einer Menge von 0,1 bis 0,6 Gew.-%, Alkalinitrat in einer von 0,05 bis 0,5 Gew.-%, Alkalisilicat in einer Menge von 0,01 bis 0,5 Gew.-% und Benztriazol in einer Menge von 0,01 bis 0,5 Gew.-%, Gewichtsprozent jeweils bezogen auf das Gewicht der Flüssigkeit.Since the corrosion inhibitors (component B) to be used according to the invention generally also have a pH-stabilizing effect, own buffer substances are no longer necessary. As a rule, a mixture of the corrosion inhibitors mentioned is used. A preferred corrosion inhibitor consists essentially of alkali metal laborate in an amount of 0.5 to 5% by weight, alkali metal benzate in an amount of 0.5 to 5% by weight, alkali metal nitrite in an amount of 0.1 to 0.6% by weight .-%, alkali nitrate in one of 0.05 to 0.5 wt .-%, alkali silicate in an amount of 0.01 to 0.5 wt .-% and benzotriazole in an amount of 0.01 to 0.5 wt .-%, weight percent based on the weight of the liquid.
Die Menge an Korrosionsinhibitor in der erfindungsgemässen Kühlflüssigkeit beträgt 2 bis 10 Gew.-%, vorzugsweise 3 bis 7 Gew.-%, bezogen auf das Gewicht der Flüssigkeit.The amount of corrosion inhibitor in the cooling liquid according to the invention is 2 to 10% by weight, preferably 3 to 7% by weight, based on the weight of the liquid.
Die Menge an Kavitationsinhibitor (Komponente C) in der erfindungsgemässen Kühlflüssigkeit beträgt 0,01 bis 3 Gew.-%, vorzugsweise 0,05 bis 1 Gew.-%, insbesondere 0,1 bis 0,5 Gew.-%, bezogen auf das Gewicht der Flüssigkeit. Die Verbindungen gemäss Formel I sind bevorzugt.
- Die erfindungsgemässe Kühlflüssigkeit kann zusätzlich zu den Komponenten A, B und C auch noch zweckmässige Additive, beispielsweise Antischaummittel, in wirksamer Mengen enthalten.
- Als Antischaummittel kommen beispielsweise höhere aliphatische Alkohole, vorzugsweise einwertige Alkohole mit 8 bis 20 C-Atomen, beispielsweise isoOctylalkohol, iso-Decylalkohol und iso-Tridecylalkohol in Betracht.
- Die wirksame Menge liegt bei 0,01 bis 1 Gew.-%, bezogen auf das Gewicht der Flüssigkeit.
- Um die Löslichkeit der Komponenten und der Additive zu erleichtern, können geringe Mengen Wasser zugesetzt werden. Die Menge an Wasser beträgt im allgemeinen 0,1 bis 1 Gew.-%, bezogen auf das Gewicht der Flüssigkeit.
- In addition to components A, B and C, the cooling liquid according to the invention can also contain useful additives, for example anti-foaming agents, in effective amounts.
- Suitable antifoams are, for example, higher aliphatic alcohols, preferably monohydric alcohols having 8 to 20 carbon atoms, for example iso-octyl alcohol, iso-decyl alcohol and iso-tridecyl alcohol.
- The effective amount is 0.01 to 1 wt .-%, based on the weight of the liquid.
- Small amounts of water can be added to facilitate the solubility of the components and additives. The amount of water is generally 0.1 to 1 wt .-%, based on the weight of the liquid.
Die Herstellung der erfindungsgemässen Kühlflüssigkeit erfolgt einfach durch Zusammenmischen der einzelnen Komponenten. Dies kann beispielsweise in einem mit Rührer ausgestatteten Behälter vorgenommen werden.The cooling liquid according to the invention is produced simply by mixing the individual components together. This can be done, for example, in a container equipped with a stirrer.
Die erfindungsgemässe Kühlflüssigkeit zeichnet sich durch eine überraschend hohe kavitations- hemmende und korrosionshemmende Wirkung aus. Da die einzelnen Komponenten der Flüssigkeit miteinanderverträglich sind, ist sie stabil auch bei relativ hohen und tiefen Temperaturen. Sie zeigt, insbesondere bei Verwendung von Antischaummitteln, geringe Schaumbildung.The cooling liquid according to the invention is characterized by a surprisingly high cavitation inhibitory and corrosion-inhibiting effect. Since the individual components of the liquid are compatible with one another, it is stable even at relatively high and low temperatures. It shows low foaming, especially when using anti-foaming agents.
Das erfindungsgemässe Kühlmittel ist vielseitig einsetzbar. Es wird vorzugsweise im Kühlkreislauf von Wärmekraftmaschinen und Pumpen, insbesondere von Verbrennungsmotoren eingesetzt. Dabei wird es zweckmässigerweise mit Wasser verdünnt, so dass es in einer Konzentration von 20 bis 45 Vol.-% vorliegt.The coolant according to the invention is versatile. It is preferably used in the cooling circuit of heat engines and pumps, in particular internal combustion engines. It is expediently diluted with water so that it is present in a concentration of 20 to 45% by volume.
Die Erfindung wird nun durch die folgenden Beispiele noch näher erläutert.The invention will now be explained in more detail by the following examples.
In den Beispielen kamen die folgenden Verbindungen gemäss Komponente C) zum Einsatz:
In der Verbindungen Nr. 3 steht R für ein C12-21-Kohlenwasserstoffgemisch aus C12 2%, C,3 5%, C14 12%, C15 18%, C16 17%, C17 16%, C18 12%, C19 9%, C20 6% und C21 3 Gew.-%, wobei der Anteil an Naphthenen 47 Gew.-% und der an Paraffinen 53 Gew.-% beträgt.In compound no.3, R represents a C 12-21 hydrocarbon mixture of C 12 2%, C, 3 5%, C 14 12%, C 15 18%, C 16 17%, C 17 16%, C 18 12%, C 19 9%, C 20 6% and C 21 3% by weight, the proportion of naphthenes being 47% by weight and that of paraffins 53% by weight.
Es wurde eine erfindungsgemässe Kühlflüssigkeit hergestellt durch Mischen der folgengen Komponenten:
Es wurde eine erfindungsgemässe Kühlflüssigkeit hergestellt durch Mischen der folgengen Komponenten:
Es wurde eine erfindungsgemässe Kühlflüssigkeit hergestellt durch Mischen der folgengen Komponenten:
Die Beispiele 4 bis 7 zeigen weitere erfindungsgemässe Kühlflüssigkeiten; die einzelnen Komponenten und ihre Anteile in Gewichtsprozent sind nachstehend zusammengefasst:
Diese Kühlflüssigkeit bestand aus den Komponenten des Beispiels 1, jedoch ohne erfindungsgemässen Zusatz von Verbindung Nr. 1:
Die Prüfung der Kühlflüssigkeiten nach den Beispielen 1 bis 8 auf ihre antikavitative Wirkung erfolgte nach den Vorschriften der Forschungsvereinigung Verbrennungskraftmaschinen E.V. Frankfurt/Main, Bundesrepublik Deutschland.
Diese Vorschriften sind in den Richtlinien zur «Prüfung der Eignung von Kühlmittelzusätzen für die Kühlflüssigkeiten von Verbrennungsmotoren», Heft R 315, Jahr 1977, beschrieben.The cooling liquids according to Examples 1 to 8 were tested for their anticavitative activity in accordance with the regulations of the Research Association for Combustion Engines EV Frankfurt / Main, Federal Republic of Germany.
These regulations are contained in the guidelines for «Prü the suitability of coolant additives for the coolants of internal combustion engines », booklet R 315, year 1977.
Entsprechend dieser Prüfmethode wurde die Gewichtsabnahme von Prüfkörpern aus der Aluminiumlegierung AICuMg2 gemessen. Je ein Prüfkörper wurde in der zu testenden Flüssigkeit in einer Ultraschallapparatur der Schwingungskavitation ausgesetzt, wobei die Schwingungsfrequenz 20 kHz ± 250 Hz und Amplitude der Schwingung am Prüfkörper 20 µm beträgt, und die Temperatur der Kühlflüssigkeit bei 80 ± 1 liegt.
- Entsprechend den genannten Vorschriften wurden jeweils 4000 ml Flüssigkeit eingesetzt, die dadurch bereitet worden ist, dass die Kühlflüssigkeit gemäss den Beispielen 1 bis 8 mit Wasser 1 : 10 verdünnt wurde. Die Prüfkörper wurden achtmal hintereinander, nach jeweils 10 Minuten Behandlung in der genannten Ultraschallapparatur, gewogen. Die Auswertung der acht Wägungen pro Prüfkörper und pro Kühlflüssigkeit erfolgte ebenfalls nach den genannten Vorschriften:
- Danach werden die ersten vier Wägungen nicht berücksichtigt. Von den restlichen vier Werten wird der höchste und der niedrigste Wert ebenfalls nicht berücksichtigt. Aus den verbleibenden zwei Werten wird das arithmetische Mittel gebildet. Dieser Gewichtswert, ausgedrückt in Milligramm pro Stunde, stellt das Testergebnis, nämlich die Gewichtsabnahme des Prüfkörpers, dar.
- In accordance with the regulations mentioned, 4000 ml of liquid were used in each case, which was prepared by diluting the cooling liquid according to Examples 1 to 8 with water 1:10. The test specimens were weighed eight times in succession, after each 10 minutes of treatment in the ultrasound apparatus mentioned. The eight weighings per test specimen and per coolant were also evaluated according to the above-mentioned regulations:
- After that, the first four weighings are ignored. The highest and lowest of the remaining four values are also not taken into account. The arithmetic mean is formed from the remaining two values. This weight value, expressed in milligrams per hour, represents the test result, namely the weight loss of the test specimen.
Nachstehend sind die Messergebnisse mit den Kühlflüssigkeiten gemäss den Beispielen 1 bis 8 zusammengefasst:
Claims (4)
the amount of the corrosion inhibitor being from 2 to 10 percent by weight and the amount of the cavitation inhibitor being from 0.01 to 3 percent by weight, percentages by weight being relative to the weight of the liquid.
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AT81107255T ATE8794T1 (en) | 1980-09-19 | 1981-09-15 | CORROSION INHIBITING AND CAVITATION INHIBITING COOLANT. |
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DE19803035327 DE3035327A1 (en) | 1980-09-19 | 1980-09-19 | COOLING LIQUID WITH CORROSION AND CAVITATION-RESISTANT ADDITIVES |
DE3035327 | 1980-09-19 |
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DE10313280A1 (en) * | 2003-03-25 | 2004-10-07 | Basf Ag | Antifreeze concentrates and coolant compositions based on polyglycols and amides for the protection of magnesium and its alloys |
WO2005006476A1 (en) | 2003-07-11 | 2005-01-20 | Shishiai-Kabushikigaisha | Cooling fluid composition for fuel battery |
US6982062B2 (en) * | 2003-07-22 | 2006-01-03 | Ashland Inc. | Corrosion inhibiting composition |
CA2546332A1 (en) * | 2003-11-13 | 2005-05-26 | Vladisav Milovanovic | The nontoxic watery solution against freezing and corrosion and the regenerator for the utilized antifreeze |
JPWO2006046275A1 (en) * | 2004-10-25 | 2008-05-22 | シーシーアイ株式会社 | Antifreeze / coolant composition |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2951038A (en) * | 1960-08-30 | Anti-freeze composition | ||
US2817636A (en) * | 1954-10-04 | 1957-12-24 | Gulf Research Development Co | Permanent type antifreeze composition |
NL104477C (en) * | 1957-03-05 | |||
US3699052A (en) * | 1969-11-12 | 1972-10-17 | Drew Chem Corp | Corrosion inhibitor composition containing a glycine,chelating agent,phosphoric or boric acid ester,and a water soluble divalent metal salt |
NL7313387A (en) * | 1973-07-02 | 1975-01-06 | Betz Laboratories | METHOD OF ANTI-CORROSION. |
BE810115A (en) * | 1973-10-30 | 1974-05-16 | CORROSION INHIBITION METHOD USING CULFONYL GLYCINE COMPOUNDS | |
DE2929413A1 (en) * | 1979-07-20 | 1981-02-05 | Hoechst Ag | CORROSION PROTECTIVE AGENT FOR ALUMINUM AND ALUMINUM ALLOYS |
-
1980
- 1980-09-19 DE DE19803035327 patent/DE3035327A1/en not_active Withdrawn
-
1981
- 1981-09-14 US US06/301,735 patent/US4404113A/en not_active Expired - Fee Related
- 1981-09-15 AT AT81107255T patent/ATE8794T1/en not_active IP Right Cessation
- 1981-09-15 EP EP81107255A patent/EP0048429B1/en not_active Expired
- 1981-09-15 DE DE8181107255T patent/DE3165246D1/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
DE3035327A1 (en) | 1982-05-06 |
DE3165246D1 (en) | 1984-09-06 |
EP0048429A1 (en) | 1982-03-31 |
US4404113A (en) | 1983-09-13 |
ATE8794T1 (en) | 1984-08-15 |
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